A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593774



Internal ID21542365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60366621..60366747hg38UCSC Ensembl
chr15:60658820..60658946hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099540
SamplesNA19238
Known GenesANXA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593774
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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